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Aminolysis of P-trichloro-N-dichlorophosphorylmonophosphazene and the crystal structure of 1-(dichlorophosphinyl)-2-chloro-2,2-bis(diisopropylamino)phosphazene

✍ Scribed by Zeynel Kılıçc; Necla Gündüz; Mustafa Yıldız; Adem Kılıçc; Sevtap Mor; Filiz Ercan; Tuncer Hökelek; Dinçer Ülkü


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
728 KB
Volume
5
Category
Article
ISSN
1042-7163

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✦ Synopsis


The reactions of Ci3P=N-P(0)C12 (1) with primary and secondary amines have been studied. The following monophosphazenes, (RRV),P= N-P(O)(NRR),, and bis(phosphinoyl)amines, [(RRN),P(O)],NH were isolated: NRR = NHCH2Ph, NEt,, NH(CH2),CH3 groups for monophosphazenes, and NEt,, NH(CH2),CH3 for phosphinoyl arnines. The unexpected geminal phosphazene, Cl(RIW),P= N-P(O)Cl,, (RIW = N[CH(CH3)?I2}, was also obtained in moderate yield. The spectral data (ZR, ' H , C , and 3iP N M R , and M S ) are presented. The structure of 1 -(dichlorophosphinyl)-2-chloro-2,2-bis(diisopro-py1amino)phosphazene (5) was determined by X-ray crystallography. The basicities of these and related compounds in nonaqueous nitrobenzene solution were obtained bv potentiometric titration.


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The Molecular and Crystal Structure of 1
✍ Dr. L. Kutschabsky; Dr. H. Dorn 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 376 KB

## Abstract The three‐dimensional structure of the title compound has been established by means of an X‐ray analysis. The product was formed by a thermal 1,3‐dipolar cycloaddition. According to the concerted [~π~4~__s__~ + ~π~2~__s__~]‐mechanism the formation of this stereoisomer should actually be